Otoferlin Gene-Mediated Hearing Loss
Otoferlin gene-mediated hearing loss is a rare genetic condition that affects the ability to hear, often resulting in profound hearing loss from birth or early childhood due to mutations in the otoferlin gene.
We are studying a new gene therapy for people with hearing loss due to Otoferlin gene mutations. The trial aims to assess the long-term safety and effectiveness of this treatment.
Health conditions and diseases that the clinical trial is designed to study and treat.
Otoferlin gene-mediated hearing loss is a rare genetic condition that affects the ability to hear, often resulting in profound hearing loss from birth or early childhood due to mutations in the otoferlin gene.
These questions help us understand your situation so we can let the trial team know whether you might be a potential match. This is not a medical evaluation and is not part of the official screening, the study doctor will make the final decision..
Experimental substances that are being investigated in this clinical trial. These are not yet approved for general use.
Locations and medical facilities where this clinical trial is currently recruiting or conducting research. Select the locations where you would like to participate.
Disclaimer: Parts of this content have been automatically extracted from the EU Clinical Trials registry. While we strive for accuracy, please always contact the trial site or sponsor directly for correct and official information before making any decisions about participation. View on EU Clinical Trials.